Optimizing feeding methods for preterm infants
How to Optimize Enteral Feeding of the Full Enteral Feeding Preterm Infant: Evaluation of Different Gastric Tube Management Practices
IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06760832
This study is testing two different ways of feeding very low-birth-weight preterm infants to see which method helps them tolerate feeding better and have fewer problems.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Sex | All |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna (other) |
| Locations | 1 site (Bologna, Bolgona) |
| Trial ID | NCT06760832 on ClinicalTrials.gov |
What this trial studies
This study evaluates different methods of enteral feeding in very low-birth-weight preterm infants who have achieved full enteral feeding. It compares intermittent gastric tube placement with permanent gastric tube maintenance to determine which method leads to better feeding tolerance and fewer adverse effects. The study will assess parameters such as gastric stagnation, cardio-respiratory events, and signs of discomfort related to tube management. The goal is to provide evidence-based recommendations for enteral feeding practices in this vulnerable population.
Who should consider this trial
Good fit: Ideal candidates are preterm infants born before 32 weeks of gestation or weighing less than 1500 grams who are receiving full enteral feeding.
Not a fit: Patients requiring invasive ventilatory support or those with congenital gastrointestinal malformations may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve feeding tolerance and reduce adverse effects in preterm infants, enhancing their overall health outcomes.
How similar studies have performed: There is currently no literature directly comparing the different modes of enteral feeding management in preterm infants, making this approach novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Gestational Age \<32 weeks and/or neonatal weight \<1500 g * Achievement of full enteral feeding (150 ml/kg/day of milk) * Exclusive feeding of human milk (breast and/or bank) * Informed consent signed by parent or legal guardian Exclusion Criteria: * Need for invasive ventilatory support * Congenital malformations affecting the gastrointestinal tract
Where this trial is running
Bologna, Bolgona
- IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna, Bolgona, Italy (RECRUITING)
Study contacts
- Principal investigator: Arianna Aceti, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Arianna Aceti, MD
- Email: arianna.aceti2@unibo.it
- Phone: 0512143779
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Preterm Birth, Feeding Methods, enteral feeding, preterm newborns, full enteral feeding